Genetic Recombination in the Lignin-Degrading Basidiomycete Phanerochaete chrysosporium.
Identifieur interne : 001055 ( Main/Exploration ); précédent : 001054; suivant : 001056Genetic Recombination in the Lignin-Degrading Basidiomycete Phanerochaete chrysosporium.
Auteurs : M. Alic [États-Unis] ; M H GoldSource :
- Applied and environmental microbiology [ 0099-2240 ] ; 1985.
Abstract
Heterokaryons made from auxotrophic strains of the lignin-degrading basidiomycete Phanerochaete chrysosporium were induced to fruit. The isolation of wild-type and double-mutant phenotypes from these crosses indicated that genetic recombination had occurred. Cytological studies demonstrated that more than 90% of the basidiospores from the wild-type and auxotrophic strains and from forced heterokaryons were binucleate. Colonies of the wild-type strain of P. chrysosporium arising from single, predominantly uninucleate conidia were all capable of producing fruit bodies and basidiospores.
DOI: 10.1128/AEM.50.1.27-30.1985
PubMed: 16346838
PubMed Central: PMC238567
Affiliations:
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Alic</name><affiliation wicri:level="2"><nlm:affiliation>Department of Chemical, Biological, and Environmental Sciences, Oregon Graduate Center, Beaverton, Oregon 97006-1999.</nlm:affiliation><country xml:lang="fr">États-Unis</country><placeName><region type="state">Oregon</region></placeName><wicri:cityArea>Department of Chemical, Biological, and Environmental Sciences, Oregon Graduate Center, Beaverton</wicri:cityArea></affiliation></author><author><name sortKey="Gold, M H" sort="Gold, M H" uniqKey="Gold M" first="M H" last="Gold">M H Gold</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1985">1985</date><idno type="RBID">pubmed:16346838</idno><idno type="pmid">16346838</idno><idno type="pmc">PMC238567</idno><idno type="doi">10.1128/AEM.50.1.27-30.1985</idno><idno type="wicri:Area/Main/Corpus">001051</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">001051</idno><idno type="wicri:Area/Main/Curation">001051</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">001051</idno><idno type="wicri:Area/Main/Exploration">001051</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Genetic Recombination in the Lignin-Degrading Basidiomycete Phanerochaete chrysosporium.</title><author><name sortKey="Alic, M" sort="Alic, M" uniqKey="Alic M" first="M" last="Alic">M. Alic</name><affiliation wicri:level="2"><nlm:affiliation>Department of Chemical, Biological, and Environmental Sciences, Oregon Graduate Center, Beaverton, Oregon 97006-1999.</nlm:affiliation><country xml:lang="fr">États-Unis</country><placeName><region type="state">Oregon</region></placeName><wicri:cityArea>Department of Chemical, Biological, and Environmental Sciences, Oregon Graduate Center, Beaverton</wicri:cityArea></affiliation></author><author><name sortKey="Gold, M H" sort="Gold, M H" uniqKey="Gold M" first="M H" last="Gold">M H Gold</name></author></analytic><series><title level="j">Applied and environmental microbiology</title><idno type="ISSN">0099-2240</idno><imprint><date when="1985" type="published">1985</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Heterokaryons made from auxotrophic strains of the lignin-degrading basidiomycete Phanerochaete chrysosporium were induced to fruit. The isolation of wild-type and double-mutant phenotypes from these crosses indicated that genetic recombination had occurred. Cytological studies demonstrated that more than 90% of the basidiospores from the wild-type and auxotrophic strains and from forced heterokaryons were binucleate. Colonies of the wild-type strain of P. chrysosporium arising from single, predominantly uninucleate conidia were all capable of producing fruit bodies and basidiospores.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">16346838</PMID><DateCompleted><Year>2010</Year><Month>06</Month><Day>25</Day></DateCompleted><DateRevised><Year>2020</Year><Month>07</Month><Day>27</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0099-2240</ISSN><JournalIssue CitedMedium="Print"><Volume>50</Volume><Issue>1</Issue><PubDate><Year>1985</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Applied and environmental microbiology</Title><ISOAbbreviation>Appl Environ Microbiol</ISOAbbreviation></Journal><ArticleTitle>Genetic Recombination in the Lignin-Degrading Basidiomycete Phanerochaete chrysosporium.</ArticleTitle><Pagination><MedlinePgn>27-30</MedlinePgn></Pagination><Abstract><AbstractText>Heterokaryons made from auxotrophic strains of the lignin-degrading basidiomycete Phanerochaete chrysosporium were induced to fruit. The isolation of wild-type and double-mutant phenotypes from these crosses indicated that genetic recombination had occurred. Cytological studies demonstrated that more than 90% of the basidiospores from the wild-type and auxotrophic strains and from forced heterokaryons were binucleate. Colonies of the wild-type strain of P. chrysosporium arising from single, predominantly uninucleate conidia were all capable of producing fruit bodies and basidiospores.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Alic</LastName><ForeName>M</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Chemical, Biological, and Environmental Sciences, Oregon Graduate Center, Beaverton, Oregon 97006-1999.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gold</LastName><ForeName>M H</ForeName><Initials>MH</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Appl Environ Microbiol</MedlineTA><NlmUniqueID>7605801</NlmUniqueID><ISSNLinking>0099-2240</ISSNLinking></MedlineJournalInfo></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1985</Year><Month>7</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1985</Year><Month>7</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1985</Year><Month>7</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16346838</ArticleId><ArticleId IdType="pmc">PMC238567</ArticleId><ArticleId IdType="doi">10.1128/AEM.50.1.27-30.1985</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Adv Genet. 1953;5:141-238</Citation><ArticleIdList><ArticleId IdType="pubmed">13040135</ArticleId></ArticleIdList></Reference><Reference><Citation>Appl Environ Microbiol. 1979 May;37(5):938-42</Citation><ArticleIdList><ArticleId IdType="pubmed">16345389</ArticleId></ArticleIdList></Reference><Reference><Citation>Science. 1983 Aug 12;221(4611):661-3</Citation><ArticleIdList><ArticleId IdType="pubmed">17787736</ArticleId></ArticleIdList></Reference><Reference><Citation>Appl Environ Microbiol. 1983 Jul;46(1):260-3</Citation><ArticleIdList><ArticleId IdType="pubmed">16346345</ArticleId></ArticleIdList></Reference><Reference><Citation>Appl Environ Microbiol. 1982 Oct;44(4):996-1000</Citation><ArticleIdList><ArticleId IdType="pubmed">16346124</ArticleId></ArticleIdList></Reference><Reference><Citation>Appl Environ Microbiol. 1978 Jun;35(6):1223-5</Citation><ArticleIdList><ArticleId IdType="pubmed">28081</ArticleId></ArticleIdList></Reference><Reference><Citation>Arch Biochem Biophys. 1984 Nov 1;234(2):353-62</Citation><ArticleIdList><ArticleId IdType="pubmed">6497376</ArticleId></ArticleIdList></Reference><Reference><Citation>Biochem Biophys Res Commun. 1983 Aug 12;114(3):1077-83</Citation><ArticleIdList><ArticleId IdType="pubmed">6615503</ArticleId></ArticleIdList></Reference><Reference><Citation>Basic Life Sci. 1981;18:19-32</Citation><ArticleIdList><ArticleId IdType="pubmed">7271709</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 1984 Apr;81(8):2280-4</Citation><ArticleIdList><ArticleId IdType="pubmed">16593451</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Oregon</li></region></list><tree><noCountry><name sortKey="Gold, M H" sort="Gold, M H" uniqKey="Gold M" first="M H" last="Gold">M H Gold</name></noCountry><country name="États-Unis"><region name="Oregon"><name sortKey="Alic, M" sort="Alic, M" uniqKey="Alic M" first="M" last="Alic">M. 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